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3,5-dichlorobenzyl piperazine-1-carboxylate synthesis

3synthesis methods
1,4-Piperazinedicarboxylic acid, 1-[(3,5-dichlorophenyl)methyl] 4-(1,1-dimethylethyl) ester

1144037-36-4
1 suppliers
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3,5-dichlorobenzyl piperazine-1-carboxylate

1144037-37-5
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Yield:1144037-37-5 93.2 %

Reaction Conditions:

with trifluoroacetic acid in dichloromethane at 20;

Steps:

3,5-dichlorobenzyl piperazine-1-carboxylate (35).

To a solution of 34 (1.95 g, 5.00 mmol) in CH2Cl2(10 mL)was added trifluoroacetic acid (5 mL).The reaction mixture was stirred at room temperature for 3 h.The solvent was evaporated to dryness.The product was neutralized with 1M K2CO3solution and extracted with ethyl acetate.The organic layer was dehydrated with anhydrous sodium sulfate and concentrated.The product was purified by amino column chromatography (hexane/ethyl acetate)to give 35 as a colorless oil (1.44 g, 93.2%).

References:

KR102502940,2023,B1 Location in patent:Paragraph 0400-0401; 0405-0407

60211-57-6 Synthesis
3,5-Dichlorobenzyl alcohol

60211-57-6
238 suppliers
$8.00/1g

3,5-dichlorobenzyl piperazine-1-carboxylate

1144037-37-5
7 suppliers
inquiry